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Peer Review reports

From: KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome

Original Submission
18 May 2015 Submitted Original manuscript
Author responded Author comments
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Reviewed Reviewer Report
Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Author responded Author comments
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
11 Aug 2015 Editorially accepted
22 Aug 2015 Article published 10.1186/s12881-015-0211-0

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